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nsv6514101

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:373

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 18 studies. See in: genome view    
    Submitted genomic45,507,901-45,508,273Question Mark
    Overlapping variant regions from other studies: 117 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):45,800,099-45,800,471Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6514101Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1545,507,90145,508,273
    nsv6514101RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1545,800,09945,800,471

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18024613deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18024613Submitted genomicNC_000015.10:g.455
    07901_45508273del
    GRCh38 (hg38)NC_000015.10Chr1545,507,90145,508,273
    nssv18024613RemappedPerfectNC_000015.9:g.4580
    0099_45800471del
    GRCh37.p13First PassNC_000015.9Chr1545,800,09945,800,471

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18024613<0.001133582
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